Impact of subcutaneous immunoglobulin on quality of life in patients with chronic inflammatory demyelinating polyneuropathy previously treated with intravenous immunoglobulin
- PMID: 34076265
- DOI: 10.1002/mus.27345
Impact of subcutaneous immunoglobulin on quality of life in patients with chronic inflammatory demyelinating polyneuropathy previously treated with intravenous immunoglobulin
Abstract
Introduction/aims: Intravenous immunoglobulin (IVIg) is a common therapy for patients with chronic inflammatory demyelinating polyneuropathy (CIDP). IVIg may cause systemic adverse events (AEs); therefore, infusion of subcutaneous immunoglobulin (SCIg) may be preferred by some patients. In this study we document the experiences of patients transitioning from IVIg to SCIg.
Methods: Transitioning subjects with CIDP were followed in a 6-month prospective, open-label study. The primary endpoint was percentage of subjects who withdrew for any reason (including significant AEs). The secondary endpoint was symptom progression or relapse requiring a change in management. Quality of life (QOL) and treatment satisfaction were assessed using the Short Form 36-item Health Survey (SF-36), Treatment Satisfaction Questionnaire for Medication (TSQM), and Chronic Acquired Polyneuropathy Patient-Reported Index (CAP-PRI). Efficacy was assessed using the Inflammatory Rasch-built Overall Disability Scale, hand-held dynamometry, limb motor strength testing (LMST), and timed 25-ft walk (T25-FW).
Results: Fifteen CIDP subjects transitioned from IVIg to SCIg. Of these, three (20%) met the primary endpoint and one (7%) met the secondary endpoint. The SF-36 showed a statistically significant improvement for the domain of role limitations-physical after 24 weeks (P = .03), with no significant differences observed in other domains. TSQM and CAP-PRI showed significant differences in favor of SCIg (P = .003 and .02, respectively). No significant differences were observed in efficacy after 24 weeks, except for LMST, which favored SCIg (P = .003). Eight of the 12 study completers (67%) continued with SCIg.
Discussion: Transition to SCIg was associated with maintained efficacy and improved QOL.
Keywords: CIDP; QOL; SCIg; immunoglobulin; patient-reported outcomes; treatment.
© 2021 Wiley Periodicals LLC.
Similar articles
-
Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (The PATH Study): study protocol for a randomized controlled trial.Trials. 2016 Jul 25;17(1):345. doi: 10.1186/s13063-016-1466-2. Trials. 2016. PMID: 27455854 Free PMC article. Clinical Trial.
-
Subcutaneous immunoglobulin as first-line therapy in treatment-naive patients with chronic inflammatory demyelinating polyneuropathy: randomized controlled trial study.Eur J Neurol. 2017 Feb;24(2):412-418. doi: 10.1111/ene.13218. Epub 2016 Dec 21. Eur J Neurol. 2017. PMID: 28000311 Clinical Trial.
-
Patient-reported outcomes with subcutaneous immunoglobulin in chronic inflammatory demyelinating polyneuropathy: the PATH study.Eur J Neurol. 2020 Jan;27(1):196-203. doi: 10.1111/ene.14056. Epub 2019 Sep 23. Eur J Neurol. 2020. PMID: 31400231 Clinical Trial.
-
Subcutaneous immunoglobulin treatment for chronic inflammatory demyelinating polyneuropathy.Muscle Nerve. 2021 Sep;64(3):243-254. doi: 10.1002/mus.27356. Epub 2021 Jul 14. Muscle Nerve. 2021. PMID: 34260074 Free PMC article. Review.
-
IgPro20, the Polyneuropathy and Treatment with Hizentra® study (PATH), and the treatment of chronic inflammatory demyelinating polyradiculoneuropathy with subcutaneous IgG.Immunotherapy. 2018 Aug;10(11):919-933. doi: 10.2217/imt-2018-0036. Epub 2018 May 16. Immunotherapy. 2018. PMID: 29764262 Review.
Cited by
-
Subcutaneous immunoglobulins (SCIG) for chronic inflammatory demyelinating polyneuropathy (CIDP): A comprehensive systematic review of clinical studies and meta-analysis.Neurol Sci. 2024 Nov;45(11):5213-5230. doi: 10.1007/s10072-024-07640-3. Epub 2024 Jun 28. Neurol Sci. 2024. PMID: 38937399 Free PMC article.
-
Toward a Sociology of Plasma Products.Int J Soc Determinants Health Health Serv. 2024 Oct;54(4):412-422. doi: 10.1177/27551938241269136. Epub 2024 Aug 14. Int J Soc Determinants Health Health Serv. 2024. PMID: 39140304 Free PMC article.
-
Patient-reported preferences for subcutaneous or intravenous administration of parenteral drug treatments in adults with immune disorders: a systematic review and meta-analysis.J Comp Eff Res. 2024 Sep;13(9):e230171. doi: 10.57264/cer-2023-0171. Epub 2024 Aug 8. J Comp Eff Res. 2024. PMID: 39115099 Free PMC article.
-
Subcutaneous Immunoglobulin in Chronic Inflammatory Demyelinating Polyneuropathy: A Historical Perspective.J Clin Med. 2023 Nov 7;12(22):6961. doi: 10.3390/jcm12226961. J Clin Med. 2023. PMID: 38002576 Free PMC article. Review.
References
REFERENCES
-
- van Schaik IN, Bril V, van Geloven N, et al. Subcutaneous immunoglobulin for maintenance treatment in chronic inflammatory demyelinating polyneuropathy (PATH): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet Neurol. 2018;17:35-46.
-
- Racosta JM, Sposato LA, Kimpinski K. Subcutaneous versus intravenous immunoglobulin for chronic autoimmune neuropathies: a meta-analysis. Muscle Nerve. 2017;55:802-809.
-
- Radinsky S, Bonagura VR. Subcutaneous immunoglobulin infusion as an alternative to intravenous immunoglobulin. J Allergy Clin Immunol. 2003;112:630-633.
-
- Lee DH, Linker RA, Paulus W, Schneider-Gold C, Chan A, Gold R. Subcutaneous immunoglobulin infusion: a new therapeutic option in chronic inflammatory demyelinating polyneuropathy. Muscle Nerve. 2008;37:406-409.
-
- Rajabally YA, Cavanna AE. Health-related quality of life in chronic inflammatory neuropathies: a systematic review. J Neurol Sci. 2015;348:18-23.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous